Skip to the page

Data / Medical devices / Accessories, Implant, Dental, Endosseous / Spain

FDA-registered makers of Accessories, Implant, Dental, Endosseous in Spain: 10 establishments

10 establishments in Spain are registered with the FDA to make Accessories, Implant, Dental, Endosseous (product code NDP). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Accessories, Implant, Dental, Endosseous
Product code
NDP
Country
Spain

Makers of Accessories, Implant, Dental, Endosseous in Spain

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Avinent Implant System S.L.U.Santpedor Barcelona, SpainManufacturer0000api.fda.gov
B.T.I. Biotechnology Institute, S.L.Miñano Alava, SpainExporter to the US, Manufacturer, Specification developer0000api.fda.gov
Ceraroot S.L.Les Franqueses del Valles Barcelona, SpainExporter to the US, Manufacturer, Specification developer0000api.fda.gov
Gmi Dental Implantology, S.L.Lleida Lerida, SpainManufacturer0000api.fda.gov
Iditec North West S.L.TORRELODONES Madrid(Autonomous Community), SpainManufacturer0000api.fda.gov
Implant Protesis Dental 2004, S.L.Premia de Dalt Barcelona, SpainManufacturer0000api.fda.gov
Mozo-Grau SAValladolid, SpainExporter to the US, Manufacturer0000api.fda.gov
Talladium Espana, SLLLEIDA Lerida, SpainManufacturer0000api.fda.gov
Terrats Medical, S.L.Barbera del Valles Barcelona, SpainContract manufacturer, Manufacturer0000api.fda.gov
Ziacom Implants SluPinto Madrid(Province), SpainComplaint file establishment, Manufacturer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.